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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → Ethyl 3-hydroxy-4-oxopiperidine-1-carboxylate

HRID 38531
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HRID 38531 반응식
[OH:1][CH:2]1[C:7](OC)([O:8]C)[CH2:6][CH2:5][N:4]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:3]1.FC(F)(F)C(O)=O>C1COCC1>[OH:1][CH:2]1[C:7](=[O:8])[CH2:6][CH2:5][N:4]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:3]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 3019465Ethyl 3-hydroxy-4,4-dimethoxypiperidine-1-carboxylate

생성물 1

HCID 58116852Ethyl 3-hydroxy-4-oxopiperidine-1-carboxylate수율 117.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Ethyl 3-hydroxy-4,4-dimethoxypiperidine-1-carboxylate from Example 34A (5.00 g, 21.4 mmol) was dissolved in THF (50 mL), and trifluoroacetic acid (15.9 mL, 214 mmol) was added. The mixture was stirred for 3.5 h at rt. The solvent was then removed in vacuo. Twice, toluene was added and again removed in vacuo. The residue was dissolved in dichloromethane, dried over sodium sulfate, and the solvent was removed in vacuo to yield 4.70 g (95%) of an oil, which was used without further purification.

후처리

  1. customThe solvent was then removed in vacuo
  2. additionTwice, toluene was added
  3. customagain removed in vacuo
  4. dissolutionThe residue was dissolved in dichloromethane
  5. dry with materialdried over sodium sulfate
  6. customthe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-0f23eb935e624549bb2a1931a2483b84
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524722B2

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